Marfan syndrome: Evolving organ manifestations—A 10‐year follow‐up study-Reference-Cited by-同舟云学术

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Marfan syndrome: Evolving organ manifestations—A 10‐year follow‐up study

Published:2019-12-11 Issue:2 Volume:182 Page:397-408
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Vanem Thy Thy¹²^ORCID,Böker Tordis¹³,Sandvik Gunhild F.¹⁴,Kirkhus Eva³,Smith Hans‐Jørgen¹³,Andersen Kai²,Drolsum Liv¹⁴,Lundby Rigmor¹³,Røe Cecilie¹⁵,Krohg‐Sørensen Kirsten¹²,Geiran Odd R.¹²,Paus Benedicte¹⁶,Rand‐Hendriksen Svend¹⁷

Affiliation:

1. Faculty of Medicine, University of OsloInstitute of Clinical Medicine Oslo Norway

2. Department of Cardiothoracic SurgeryOslo University Hospital (OUH) Oslo Norway

3. Department of Radiology and Nuclear MedicineOUH Oslo Norway

4. Department of OphthalmologyOUH Oslo Norway

5. Department of Physical Medicine and RehabilitationOUH Oslo Norway

6. Department of Medical GeneticOUH Oslo Norway

7. TRS, National Resource Centre for Rare DisordersSunnaas Rehabilitation Hospital Nesoddtangen Norway

Funder

Roy Magnus Løkens Foundation for Medical Imaging

TRS, National Resource Centre for Rare Disorders

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61441

Reference54 articles.

1. Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes

2. Noninvasive diagnosis and management of spontaneous intracranial hypotension in patients with marfan syndrome: Case Report and Review of the Literature

3. Fatigue in adults with Marfan syndrome, occurrence and associations to pain and other factors

4. MRI measurements of the thoracic aorta and pulmonary artery

5. Dural ectasia in Marfan syndrome and other hereditary connective tissue disorders: a 10-year follow-up study

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1. Impact of valve-sparing aortic root replacement on aortic fluid dynamics and biomechanics in patients with syndromic heritable thoracic aortic disease;Journal of Cardiovascular Magnetic Resonance;2024-08

2. Ventricular arrhythmias in a child with Marfan syndrome: case report;Journal of Arrhythmology;2024-05-30

3. Quantitative measurement of dural ectasia: associations with clinical and genetic characteristics in Marfan syndrome;European Spine Journal;2024-04-14

4. The role of musculoskeletal aspects in the early diagnosis of Marfan Syndrome in children;Minerva Orthopedics;2022-10

5. Marfan syndrome and adolescent idiopathic scoliosis patients have similar 90-day postoperative outcomes and 5-year reoperation rates after spinal deformity surgery;Spine Deformity;2022-04-01

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